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PLEASE READ ALL PARTS OF THE QUESTION AND REQUIREMENTS CAREFULLY  ***Answers that fail to meet all the requirements outlined below will NOT receive full credit*** Answer This Long Essay Question (1 of 1): Thomas Paine proclaimed in 1776 that the American revolutionary democratic project aimed to “begin the world over again.” As we have seen, Americans from all backgrounds have, over the nation’s history, tried to do just that for their own ends and to achieve more of the promises enshrined in the U.S.’s foundational documents. Consider these ideas and ideals in terms of how understandings of American freedom have evolved since the Revolution. How have different — and changing — meanings of freedom shaped the nation’s democratic traditions from the founding to the present? Requirements: In developing your essay, you must use at least four (4) primary-source documents from the course as evidence to support your arguments. In your answer, you must refer to at least one document from each of the three (3) centuries the course covered (so at least one from the 1700s, 1800s, and 1900s).  

Determine if the following statement is True or False:   Progressives hoped to accomplish their reformist agenda by relying exclusively on the power of the federal government

You have arrived at the Bonus Question! Please only complete this question once you have finished all other sections to the best of your ability. 

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Graph the function. Be sure to label all asymptotes. If none exist, write none. Lisa the domain (use interval notation) and the x- and y- intercept(s). Remember, intercepts are ordered pairs and asymptotes are equations. (2 pts each questions, 3 pts for the graph)

On the answer sheet provided to you for the exam, or on scrap paper, complete the following question: Written Response Question 3 (12 pts):  Complete the following reactions showing the major organic product or products. Click to Show Image Description A reaction scheme centers on a branched acyl chloride. Its carbonyl carbon is double-bonded to O, single-bonded to Cl, and bonded to a carbon with two terminal carbon bonds. Four lines extend diagonally to outward-pointing reaction arrows. The upper-left arrow is labeled “2 CH₃NH₂.” The upper-right arrow is labeled “1) DIBAH” and “2) dil. H₃O⁺.” The lower-left arrow shows CH₃C(=O)ONa. The lower-right arrow shows a two-carbon chain ending in OH above the arrow and “pyridine” below it.

Written Response/Drawing Questions Instructions The next four questions are Written Response 1 through 15. These are separate from the Canvas question numbering because you will write or draw your answers by hand. Use the CHEM 212 Exam 3 Answer Sheet if you printed it or copied it onto your own paper before the exam. If not, use blank scrap paper. You may not print the answer sheet during the exam. Clearly number each handwritten answer so it matches the written response question. After you complete Written Response 15, continue with the rest of the Canvas exam, beginning with Question 2. Do not upload your handwritten work during the exam. You will submit it after you have fully completed the exam.

The malonic ester synthesis can be adapted to synthesize a-amino acids by using diethyl acetamidomalonate as the starting material. Select the structure of the amino acid produced by the following synthesis. Click to Show Image Description A reaction scheme shows the starting compound labeled “Diethyl acetamidomalonate,” with the condensed structure CH₃–C(=O)–NH–CH(CO₂Et)₂. A right-pointing arrow lists three sequential conditions: 1. NaOEt; 2. C₆H₅CH₂Br; and 3. H₃O⁺, Δ. No product structure appears after the arrow.

Which nucleophile will not readily react with the following compound to create a more energetically favorable product?  Click to Show Image Description A five-membered line-angle ring contains an oxygen atom at the top and four carbon atoms. The ring oxygen is single bonded to a carbon on each side. Each of these two carbons is double bonded to an oxygen atom outside the ring, with one double bond extending to the left and the other extending upward and to the right. The remaining two carbon atoms form the lower portion of the ring.